A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225316



Internal ID22368485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109293353..109293788hg38UCSC Ensembl
chr13:109945701..109946136hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2429n152
Supporting Variantsnssv14368600
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225316
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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